US2366129A

US2366129A - Water-soluble resinous products and process of making

Info

Publication number: US2366129A
Application number: US453553A
Authority: US
Inventors: John B Rust
Original assignee: Montclair Research Corp
Current assignee: Montclair Research Corp
Priority date: 1942-08-04
Filing date: 1942-08-04
Publication date: 1944-12-26
Anticipated expiration: 1961-12-26

Description

Patented Dec. 26, 1944 WATER SOLUBLE RESINOUS PRODUCTS AND PROCESS OF MAKING John B. Rust, Verona, N. 8., assignor to Montclalr Research Corporation, a corporation of New Jersey No Drawing. Application August 4, 1942,

Serial No. 458,558

. .11 Claims. Y, (Cl. zeo ro) The present invention relates to water-soluble resinous products and the process of making same. It is an object of this invention to produce water-soluble resinous materials having varying degrees of hygroscopicity and which may be employed as oil-proof coatings and cements, agricultural sprays, water paints, cosmetic preparations, paper and textile sizings, adhesives, leather and rubber coatings and the like. Furthermore, the products of the present invention in some cases may be used as flame retarders. Itis a further object of thisinvention to provide resinous materials which are either permanently watersoluble or, it desired, may be cured on the application-oi heat to insoluble infusible masses.

In the process of .the present. invention an amino compound is heated with a polyfunctional inorganic acid such as boric, o-phosphoric, pyro'-- phosphoric acids and the like to first produce polyamino borates, phosphates, etc., whichare dehydrated on further heating to yield resinous bodies readily soluble in water and which may be used as indicated above. Furthermore, the poly-' amine bor ates, phosphates; etc., or their dehydration products may be heated with nitrogenous material such as urea or the urea derivatives. Thus, a resinous material is formed by heating 1 tetraethylene pentamine borate with dieyanodiamide to 210 C. The resin so obtained is infusible but may be dissolved in water. The water solutions of these urea-, or urea derivative-fusion products may be further reacted, if desired, with c an aldehyde such as formaldehyde to yield materials which can be rendered insoluble on denydration and further application of heat.

' In the present invention as the amino compound I preier to employ amines of the general type represented by NI-nwmcimm) "H (where n is an'integer less than 6) such as ethy1enedi amine, diethylenetriamine, triethylene tetramine, tetraethylenepentamine and the like, or amino compounds such as diethanol amine, trishydroxymethylaminomethane, z-amino-z-methyl- 1,8-propanediol and the like. As the inorganic acid component I preier to employ boric acid, pyroborlc acid, boric auhydride, or ortho-, meta-,

- pyroand hypophosphorlc or phosphorus acids.

I! it is desired to form the nitrogenous derivatives of the polyamino-inorganic products of the present invention, I may employ urea, guanidine,

dicyandiamide. biguanide, guanyl ureaand the The following examples are given to illustrate the products 01 the present invention and the '65 fluxed at boiling for 30 minutes. When cool the process whereby they are obtained. All proportions are in parts by weight.

Example 1.-20 parts .0! tetraethylenepentamine were mixed with 20 parts of boric acid and heated slowlyto 180C.- A clear melt was first obtained which gradually increased in viscosity as water was eliminated. After heating for about 30 minutes at 180 C. the melt was poured and a pale yellow, hard, brittle, water-soluble resin was 10 secured when cooled.

Example-2. 48.!) parts of tetraethylenepentamine were mixedwith 19 parts of 85% o-phosphoric acid. A solid tetraethylenepentammonium phosphate was obtained with evolution of heat.

is The material was heated up to 190-200. c. for

about 80 minutes. Water was eliminated and the melt increased in viscosity. On cooling a hard, brittle, pale yellow water-solubl e-resin was secured.

20 Example 3.1'l.2 parts of tetraethylenepentamine, 10.3 parts or boric acid and 42 parts or dicyandiamide were heated together with stirring to 170 C. An exothermic reaction occurred raising the temperature to 220 C. The resinous melt increased in viscosity rapidly, finally hardening and swelling to a vesiculated mass. When cool the mass was broken up. It was a white non-hygroscopic powder, soluble in water.

parts oi the above resinous material were 30 dissolved in 32 parts of water and 38 parts of 3'l%% aqueous formaldehyde solution. The solution was boiled under a reflux condenser for 30 minutes. when cool the solution was pale yellow and viscous. The solution on drying in films and 85 heating to 100-150 C. yielded water-insoluble coatings. The solution was very stable at ordinary temperatures and could be used as an adhesive, textile size and the like.

' Example 1-15 parts of tetraethylenepenta- 40 mine and 15 parts 0! pyrophosphoric acid were heated together to 180 C. ior 20 minutes with the elimination of water. On cooling a hard,

brittle, pale yellow water-soluble resin was se-.

cured.

Ezample.5.14.6 parts of triethylene tetracosity. A hard, brittle, pale colored watersoluble resin was secureda The resin as described above'was dissolved in 40 parts of water and 30 parts or 37 aqueous formaldehyde solution. The solution was resolution had a light viscosity and was very stable. n pouring onto a plate and heating, the solution dried and cured to a water-insoluble film.

Example 6.11 parts of triethylene tetramine,

11 parts of o-phosphoric acid and 21 parts of di- 0 cyandiamide were heated up to 220 ,C. During heating the melt increased rapidly in viscosity and finally swelled to a hard, vesiculated mass. This was broken up on cooling to give a white, water-soluble powder. non-tacky film on drying.

To 15 parts of the above phosphorylated resin, 20 parts of 37 /2% aqueous formaldehyde solution and 65 parts of water were added. The solution was heated under a reflux condenser at boiling for about 30 minutes. A pale yellow non-viscous solution resulted, which could be cured to waterinso luble films.

Example 7.-12.1 parts of trishydroxymethyl aminomethane and 6.2 parts of boric acid were mixed and heated. The temperature was taken slowly up to 210 C. when a melt was formed. Heating was continued until foaming stopped. There was obtained a pale yellow, very high melting, non-hygroscopic resin which was watersoluble. A solution of thi resin dried to clear, white, non-tacky film. 1

The resin was useful as textile size, adhesive, water paint and the like.

Example 8.21 parts of 2-amino-2-methyl-1,3-

propanediol and 12.4 parts of boric acid were mixed and heated. The melt rapidly became viscous and foamed considerably. The temperature was raised to 215 C. slowly and heating continued until foaming had ceased or for about 20 minutes. A pale, clear, hard, rather high melting,

A water solution gave a 220 c,: an amine of formula N'Hz(CH2CH2NI-I)nI-I where n is an integer less than 6, a polyfunctional water-soluble reaction product which may be cured by application of heat.

2. Process of making water-soluble resin comprising heating tetraethylenepentamine with boric acid at 180-220 C. with the elimination of water.

until a fusible resinis secured.

3. Process of making water-soluble resin comprising heating tetraethylene pentamine, boric acid and dicyandiamide to 220 C., dissolving said reaction product in water and heating with formaldehyde to secure a water-soluble reaction product which may be cured on application of heat.

4. Process of making water-soluble resin comprising heating triethylene tetramine, boric acid, and urea to 220 C., dissolving said reaction product in water, heating with formaldehyde to obtain a water-soluble reaction product which may be cured to a water-insoluble form by application of heat.

5. Process of making water-soluble resin comprising heating tetraethylenepentamine with phosphoric acid at 180-220 C. with the elimination of water'until a fusible resin i secured.

6. Process of making water-soluble resin comprising heating tetraethylenepentamine, phosphoric acid and dicyandiamide to 220 C., dissolving said reaction product in water and heating with formaldehyde to secure a water-soluble reaction product which may be cured on application of heat.

7. Water-soluble resin comprising the reaction product of formaldehyde upon the product obtained by reacting: an amine of formula where n is an integer less than 6, a polyfunctional inorganic acid selected from the group consisting of boric and phosphoric acids,-and a, nitrogenous compound selected from the group consisting of tion product of tetraethylenepentamine and boric acid formed at 180-220 C. with the elimination of water. Y

9. Water-soluble resin comprising the reaction product of tetraethylenepentamine and phosphoric acid formed at l-220 C..with the elimination of water. c

10. Water-soluble resin comprisingthe reaction product of formaldehyde upon the product obtained by reacting: tetraethylenepentamine, boric acid and dicyandiamide, the latter product being formed at -220 C. and with elimination of water.

l1. Water-soluble resin comprising the reaction product of formaldehyde upon the product obtained by reacting: tetraethylenepentamine, phosphoric acid and dicyandiamide, the latter product being formed at 180-220 C..and with elimination of water. I

' JOHN B. RUST.